| 1. | Abnormal expansion in cgg repeats of fmr1 were not detected on 23 members of the xlmr families
2 。 23名家系成员中均未发现fmri基因cgg重复异常扩增。 |
| 2. | Unstable transmission within the cgg repeats less than 43 were found in the detection
发现fm基因cgg重复次数在低于临界值（ nm43 ）时也存在不稳定传递现象。 |
| 3. | Cgg office also provides consultation and support services to schools and organizations willing to establish farming activities
本单位亦为有意开展耕作活动之团体及学校提供意见及援助，有意者请与本单位联络。 |
| 4. | Southern blot can be performed to analyze the expansion of the cgg repeat as well , while the fmrp antibody test allows rapid detection of male patients
Fmrp抗体检测也是诊断脆性x综合征的快捷方法，但是，这几种方法均有一定的局限性。 |
| 5. | Cgg office ' s facilities including experiment field , greenhouse , composting demonstration yard , presentation barn , conference room and a small garden
有机种植社群办公室设备包括实验田、已获认证之环控温室、堆肥示?棚、演讲室、会议室及花园。 |
| 6. | Seeds , nursery service , organic fertilizers , biological pesticides and other agriculture accessories are available for sale in cgg office . please contact us for arrangement
办公室其他一般服务包括种子发售、种苗代育、有机肥料、生物农药及其他有机农业用品发售，如欲购买请先来电查询。 |
| 7. | In the normal population , the number of cgg repeats in fmr1 is highly polymorphic with the variation ranging from 6 to 54 . such statistical data are obtained from caucasia people
Fmri基因cgg重复次数在正常人中呈高度多态性，变异范围n 6 sd ，这一变异在正常人群体中的分布情况的统计数据主要来自高加索人群体。 |
| 8. | Fxs is mainly caused by a kind of dynamic mutation , the expansion of a cgg repeat located in the 5 ' - untranslated region ( 5 ' - utr ) of the fmr1 ( fragile x mental retardation ) gene
该综合症由患者细胞中可见xq27 . 3的脆性位点fraxa而得名。绝大多数脆性x综合征患者的发病是由于fmr1基因5端非翻译区的三核苷酸cgg重复的不稳定扩增所致。 |
| 9. | Therefore in order to detect the carriers in the population and fxs patients with full mutation exactly , it will be very helpful to study the variable distribution of cgg repeats of fmr1 in chinese
准确掌握中国人群中该重复序列的变异分体情况，有助于进一步对脆性x综合征进行前突变和全突变的诊断及对群体中携带者的检出提供有意义的依据。 |
| 10. | To detect the patients and carriers of the fragile x syndrome , various analytic methods could be used . one is cytogenetic diagnosis to observe the expression of the fragile site fraxa located at xq27 . 3
对脆x综合征的诊断，可以通过细胞遗传学方法观察分析x染色体相应脆性位点的表达情况，或是通过southern印迹杂交的方法直接分析cgg重复的扩增突变。 |
